K252412
- 510(k) number
- K252412
- Device name
- Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator)
- Applicant
- Applied Medical Resources Corporation CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-31
- Date received
- 2025-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252412.pdf
Official FDA record: K252412
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.